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OpenTrials
Completed

NCT Number: NCT02707159

Circulating Tumor Cells as Tools for Therapy Response in Nab-paclitaxel Treated Metastatic Pancreatic Cancer Patients

The majority patients diagnosed with pancreatic cancer have metastatic disease at the time of diagnosis. The prognosis is extremely poor with a 5-year survival rate of less than 5%. Treatment with chemotherapy can improve efficacy, but still the median progression-free survival in patients receiving nab-paclitaxel and gemcitabine is only 5,5 months and median overall survival is less than one year. There is a urgent need for tools for predicting the efficacy of the treatment. The current trial aims at investigating the biomarker potential of circulating tumor cells (CTCs) in metastatic pancreatic cancer patients treated by gemcitabine and nab-paclitaxel.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female > 18 years up to 80 years
  • Histologically or cytologically proven adenocarcinoma of the pancreas before start of treatment. Also patients for whom there is a strong suspicion of unresectable pancreatic cancer will before the diagnosis is confirmed be asked for consent to take 2 additional biopsies at the time of diagnostic biopsy retrieval, in case the histological analysis confirms that they can be included.
  • Locally advanced (primarily unresectable) and/or metastatic disease.
  • Presence of at least one measurable lesion according to the RECIST criteria, not restricted to previously irradiated area or limited to bone, pleural effusion or ascites.
  • ECOG/WHO performance status ≤2
  • Absolute neutrophil count (ANC) >1.5 x 109 /L and platelet count >100 x 109/L
  • Total bilirubin < 1.5 times the upper limit of the normal range at the institution (ULN) or AST or ALT < 2 x ULN. If liver metastases are present, patients can be included if total bilirubin < 5× ULN or AST/ALT <10× ULN. Dose reductions of paclitaxel will be performed when bilirubin >2xULN, depending on increase of the bilirubin level according to the recommendations of the Summary of Product Characteristics.
  • Serum creatinin < 1,5 ULN / calculated creatine clearance > 60 ml/min.
  • Written informed consent

Exclusion criteria

  • Current infection, bowel obstruction or subobstruction, or other uncontrolled intercurrent illness.
  • Prior medical treatment for advanced pancreatic cancer
  • Confirmed brain metastasis.
  • Concurrent or past history of another malignancy except curatively treated non-melanoma skin cancer or in situ carcinoma of the cervix.
  • Treatment with any other investigational drug more than 30 days prior to study entry.
  • Allergy to anyone of the included drugs.
  • Female patient breast feeding or pregnancy
  • Not able/ or not willing to use adequate contraception (defined below). A pregnancy test will be included in the baseline visit for women of childbearing potential.

Treatment and study plan

Nab paclitaxel / gemcitabine

Drug

Patients will receive gemcitabine/nab-paclitaxel combination chemotherapy

Other names: Nab-paclitaxel and Gemcitabine

Primary outcomes

  1. Change in levels of circulating tumor cells (CTCs) during treatment

    Time frame: Baseline and 9 months

Secondary outcomes

  1. Post-baseline over-all survival

    Time frame: Baseline and 9 months

  2. Post-baseline disease-specific survival

    Time frame: Baseline and 9 months

  3. Post-baseline time to progression

    Time frame: Baseline and 9 months

  4. Clinical response to treatment by RECIST 1.1

    Time frame: Baseline and 9 months

    Radiologic, clinical and biochemical assessment

  5. Changes in quality of life during treatment

    Time frame: Baseline and 9 months

    Quality of Life is assessed every 4 weeks during treatment and then every 8th weeks.

Sponsors and collaborators

Lead sponsor

Helse Stavanger HF

Other Gov

Registry information

Official study title

A Novel Therapy for Locally Advanced and Metastatic Pancreatic Cancer Based on Nanoparticle Albumin-bound Paclitaxel and Gemcitabine: Circulating Tumor Cells as a Potential Biomarker for Treatment Monitoring, -Response and Survival

Acronym: PACT-ACT-v6

Important dates

Study start
2014
Primary completion
2017
Study completion
2019
First posted
Mar 14, 2016
Registry last updated
Mar 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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